المؤلفون: Heckman M. G., Elbaz A., Soto-Ortolaza A. I., Serie D. J., Aasly J. O., Annesi G., Auburger G., Bacon J. A., Boczarska-Jedynak M., Bozi M., Brighina L., Chartier-Harlin M. -C., Dardiotis E., Destee A., Ferrarese C., Ferraris A., Fiske B., Gispert S., Hadjigeorgiou G. M., Hattori N., Ioannidis J. P. A., Jasinska-Myga B., Jeon B. S., Kim Y. J., Klein C., Kruger R., Kyratzi E., Lin C. -H., Lohmann K., Loriot M. -A., Lynch T., Mellick G. D., Mutez E., Opala G., Park S. S., Petrucci S., Quattrone A., Sharma M., Silburn P. A., Sohn Y. H., Stefanis L., Tadic V., Tomiyama H., Uitti R. J., Valente E. M., Vassilatis D. K., Vilarino-Guell C., White L. R., Wirdefeldt K., Wszolek Z. K., Wu R. -M., Xiromerisiou G., Maraganore D. M., Farrer M. J., Ross O. A.

المساهمون: Heckman, M. G., Elbaz, A., Soto-Ortolaza, A. I., Serie, D. J., Aasly, J. O., Annesi, G., Auburger, G., Bacon, J. A., Boczarska-Jedynak, M., Bozi, M., Brighina, L., Chartier-Harlin, M. -C., Dardiotis, E., Destee, A., Ferrarese, C., Ferraris, A., Fiske, B., Gispert, S., Hadjigeorgiou, G. M., Hattori, N., Ioannidis, J. P. A., Jasinska-Myga, B., Jeon, B. S., Kim, Y. J., Klein, C., Kruger, R., Kyratzi, E., Lin, C. -H., Lohmann, K., Loriot, M. -A., Lynch, T., Mellick, G. D., Mutez, E., Opala, G., Park, S. S., Petrucci, S., Quattrone, A., Sharma, M., Silburn, P. A., Sohn, Y. H., Stefanis, L., Tadic, V., Tomiyama, H., Uitti, R. J., Valente, E. M., Vassilatis, D. K., Vilarino-Guell, C., White, L. R., Wirdefeldt, K., Wszolek, Z. K., Wu, R. -M., Xiromerisiou, G., Maraganore, D. M., Farrer, M. J., Ross, O. A.

مصطلحات موضوعية: genetic, interaction, lrrk2, mapt, parkinson's disease, snca, adolescent, adult, aged, 80 and over, asian continental ancestry group, european continental ancestry group, female, genetic predisposition to disease, genotype, haplotype, human, leucine-rich repeat serine-threonine protein kinase-2, male, middle aged, parkinson disease, protein-serine-threonine kinase, risk, young adult, alpha-synuclein, tau protein, genetic variation

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/23962496; info:eu-repo/semantics/altIdentifier/wos/WOS:000326898400030; volume:35; issue:1; firstpage:1; lastpage:10; numberofpages:10; journal:NEUROBIOLOGY OF AGING; http://hdl.handle.net/11573/1383082Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84885187895

الإتاحة: https://doi.org/10.1016Test/j.neurobiolaging.2013.07.013
http://hdl.handle.net/11573/1383082Test

المؤلفون: Ross, O, Soto Ortolaza, A, Heckman, M, Aasly, J, Abahuni, N, Annesi, G, Bacon, J, Bardien, S, Bozi, M, Brice, A, Brighina, L, Van Broeckhoven, C, Carr, J, Chartier Harlin, M, Dardiotis, E, Dickson, D, Diehl, N, Elbaz, A, FERRARESE, CARLO, Ferraris, A, Fiske, B, Gibson, J, Gibson, R, Hadjigeorgiou, G, Hattori, N, Ioannidis, J, Jasinska Myga, B, Jeon, B, Kim, Y, Klein, C, Kruger, R, Kyratzi, E, Lesage, S, Lin, C, Lynch, T, Maraganore, D, Mellick, G, Mutez, E, Nilsson, C, Opala, G, Park, S, Puschmann, A, Quattrone, A, Sharma, M, Silburn, P, Sohn, Y, Stefanis, L, Tadic, V, Theuns, J, Tomiyama, H, Uitti, R, Valente, E, van de Loo, S, Vassilatis, D, Vilariño Güell, C, White, L, Wirdefeldt, K, Wszolek, Z, Wu, R, Farrer, M.

المساهمون: Ross, O, Soto Ortolaza, A, Heckman, M, Aasly, J, Abahuni, N, Annesi, G, Bacon, J, Bardien, S, Bozi, M, Brice, A, Brighina, L, Van Broeckhoven, C, Carr, J, Chartier Harlin, M, Dardiotis, E, Dickson, D, Diehl, N, Elbaz, A, Ferrarese, C, Ferraris, A, Fiske, B, Gibson, J, Gibson, R, Hadjigeorgiou, G, Hattori, N, Ioannidis, J, Jasinska Myga, B, Jeon, B, Kim, Y, Klein, C, Kruger, R, Kyratzi, E, Lesage, S, Lin, C, Lynch, T, Maraganore, D, Mellick, G, Mutez, E, Nilsson, C, Opala, G, Park, S, Puschmann, A, Quattrone, A, Sharma, M, Silburn, P, Sohn, Y, Stefanis, L, Tadic, V, Theuns, J, Tomiyama, H, Uitti, R, Valente, E, van de Loo, S, Vassilatis, D, Vilariño Güell, C, White, L, Wirdefeldt, K, Wszolek, Z, Wu, R, Farrer, M

مصطلحات موضوعية: Young Adult, Polymorphism, Single Nucleotide, Gene Frequency, Exon, Human, Aged, Protein-Serine-Threonine Kinase, Genome-Wide Association Study, Genotype, International Cooperation, Parkinson Disease, 80 and over, Ethnic Group, Risk Factor, Adult, Case-Control Studie, Middle Aged, Genetic Predisposition to Disease, Adolescent, Male, Female

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/21885347; info:eu-repo/semantics/altIdentifier/wos/WOS:000295814600011; volume:10; issue:10; firstpage:898; lastpage:908; numberofpages:11; journal:LANCET NEUROLOGY; http://hdl.handle.net/10281/33182Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-80052967403

الإتاحة: https://doi.org/10.1016/S1474-4422Test(11)70175-2
http://hdl.handle.net/10281/33182Test

المؤلفون: Ross, Owen A, Soto-Ortolaza, Alexandra I, Brighina, Laura, Riess, Olaf, Klein, Christine, Djarmati, Ana, Hagenah, Johann, Lohmann, Katja, van de Loo, Simone, Abahuni, Nadine, Gispert-Sánchez, Suzana, Hilker, Rüdiger, Auburger, Georg, Van Broeckhoven, Christine, Xiromerisiou, Georgia, Tsimourtou, Vaia, Ralli, Styliani, Kountra, Persa, Markou, Katerina, Patramani, Gianna, Vogiatzi, Christina, Lynch, Tim, Gibson, J Mark, Craig, Dr David, Carr, Jonathan, Valente, Enza Maria, Ferraris, Alessandro, Bentivoglio, Anna Rita, Ialongo, Tamara, Guidubaldi, Arianna, Piano, Carla, Ferrarese, Carlo, Tarantino, Patrizia, Annesi, Ferdinanda, Chartier-Harlin, Marie-Christine, Annesi, Grazia, Quattrone, Aldo, Hattori, Nobutaka, Tomiyama, Hiroyuki, Funayama, Manabu, Yoshino, Hiroyo, Li, Yuanzhe, Imamichi, Yoko, Toda, Tatsushi, Satake, Wataru, Dardiotis, Efthimios, Aasly, J., Opala, Grzegorz, Jasinska-Myga, Barbara, Boczarska-Jedynak, Magdalena, Tan, Eng King, Bardien, Soraya, Jeon, Beom Seok, Park, Sung Sup, Kim, Yun Joong, Dickson, Dennis W, Sohn, Young Ho, Belin, Andrea Carmine, Olson, Lars, Galter, Dagmar, Westerlund, Marie, Sydow, Olof, Pedersen, Nancy L, Wirdefeldt, Karin, Nilsson, Christer, Puschmann, Andreas, Diehl, Nancy N, Wu, Ruey-Meei, Maraganore, Demetrius M, Ahlskog, Eric, de Andrade, Mariza, Lesnick, Timothy G, Rocca, Walter A, Checkoway, Harvey, Farrer, M., Elbaz, Alexis, Heckman, Michael G, Fiske, Brian, Gibson, Rachel, Hadjigeorgiou, Georgios M, Ioannidis, John P A, Jeon, Beom S, Aasly, Jan O, Kruger, Rejko, Kyratzi, Elli, Lesage, Suzanne, Lin, Chin-Hsien, Lynch, Timothy, Mellick, George D, Mutez, Eugénie, Sharma, Manu, Silburn, Peter A, Stefanis, Leonidas, Tadic, Vera, Theuns, Jessie, Uitti, Ryan J, Vassilatis, Demetrios K, Vilariño-Güell, Carles, White, Linda R, Wszolek, Zbigniew K, Farrer, Matthew J, Bacon, Justin A, Disease, Genetic Epidemiology Of Parkinson's, Sutherland, G. T., Siebert, G. A., Nuytemans, Karen, Meeus, Bram, Crosiers, David, Pickut, Barbara, Engelborghs, Sebastiaan, De Deyn, Peter P, Cras, Patrick, Rogaeve, Ekaterina, Destée, A., Agid, Y., Anheim, M., Bonnet, A-M, Borg, M., Bozi, Maria, Brice, A., Broussolle, E., Corvol, J. C., Damier, P., Dürr, A., Durif, F., Lesage, S., Lohmann, E., Pollak, P., Brice, Alexis, Rascol, O., Tison, F., Tranchant, C., Viallet, F., Vidailhet, M., Gasser, Thomas, Krüger, Rejko, Berg, Daniela, Schulte, Claudia

المساهمون: Ross, O, Soto Ortolaza, A, Heckman, M, Aasly, J, Abahuni, N, Annesi, G, Bacon, J, Bardien, S, Bozi, M, Brice, A, Brighina, L, Van Broeckhoven, C, Carr, J, Chartier Harlin, M, Dardiotis, E, Dickson, D, Diehl, N, Elbaz, A, Ferrarese, C, Ferraris, A, Fiske, B, Gibson, J, Gibson, R, Hadjigeorgiou, G, Hattori, N, Ioannidis, J, Jasinska Myga, B, Jeon, B, Kim, Y, Klein, C, Kruger, R, Kyratzi, E, Lesage, S, Lin, C, Lynch, T, Maraganore, D, Mellick, G, Mutez, E, Nilsson, C, Opala, G, Park, S, Puschmann, A, Quattrone, A, Sharma, M, Silburn, P, Sohn, Y, Stefanis, L, Tadic, V, Theuns, J, Tomiyama, H, Uitti, R, Valente, E, van de Loo, S, Vassilatis, D, Vilariño Güell, C, White, L, Wirdefeldt, K, Wszolek, Z, Wu, R, Farrer, M, Engelborghs, Sebastiaan, De Deyn, Peter Paul, Cras, Patrick, Genetic Epidemiology Of Parkinson's Disease (GEO-PD) Consortium, Pathologic Biochemistry and Physiology, Pollak, Pierre

المصدر: The lancet neurology
The lancet / Neurology 10(10), 898-908 (2011). doi:10.1016/S1474-4422(11)70175-2
The Lancet Neurology, Vol. 10, No 10 (2011) pp. 898-908

مصطلحات موضوعية: Male, Polymorphism, Single Nucleotide/*genetics, International Cooperation, Ethnic Groups/genetics, Ethnic Group, Genome-wide association study, Protein-Serine-Threonine Kinase, methods [Genome-Wide Association Study], genetics [Ethnic Groups], 0302 clinical medicine, Gene Frequency, genetics [Parkinson Disease], Risk Factors, Exons/genetics, Ethnicity, Parkinson Disease/genetics, Medicine(all), Genetics, Aged, 80 and over, 0303 health sciences, Parkinson Disease, Exons, genetics [Exons], Middle Aged, Polymorphism, Single Nucleotide/genetics, Protein-Serine-Threonine Kinases, LRRK2, 3. Good health, genetics [Polymorphism, Single Nucleotide], Genome-Wide Association Study/methods, Female, Case-Control Studie, Human, Adult, Parkinson Disease/*genetics, Genotype, Adolescent, Protein-Serine-Threonine Kinases/*genetics, Protein-Serine-Threonine Kinases/genetics, Exon, Protein Serine-Threonine Kinases, Biology, Leucine-Rich Repeat Serine-Threonine Protein Kinase-2, genetics [Protein-Serine-Threonine Kinases], Polymorphism, Single Nucleotide, 03 medical and health sciences, Young Adult, Humans, Genetic Predisposition to Disease, ddc:610, LRRK2 protein, human, Risk factor, Allele frequency, 030304 developmental biology, Aged, Risk Factor, Case-control study, Exons/*genetics, Odds ratio, nervous system diseases, ddc:616.8, Minor allele frequency, Genetic epidemiology, Case-Control Studies, Neurology (clinical), Human medicine, 030217 neurology & neurosurgery, Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c760baf6e72eae84c3dd69f2ee368f5Test
http://hdl.handle.net/10281/33182Test

المؤلفون: Engelsen B. A., Tzoulis C., Karlsen B., Lillebo A., Laegreid L. M., Aasly J., Zeviani M., Bindoff L. A.

المساهمون: Engelsen, B. A., Tzoulis, C., Karlsen, B., Lillebo, A., Laegreid, L. M., Aasly, J., Zeviani, M., Bindoff, L. A.

مصطلحات موضوعية: Epilepsy, Mitochondrial disease, Occipital lobe, POLG, Status epilepticu, Adolescent, Adult, Age of Onset, Anticonvulsant, Brain, Child, DNA Polymerase gamma, DNA-Directed DNA Polymerase, Disease Progression, Electroencephalography, Epilepsies, Partial, Female, Human, Magnetic Resonance Imaging, Male, Middle Aged, Prognosi, Syndrome, Mutation

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/18238797; info:eu-repo/semantics/altIdentifier/wos/WOS:000253489800022; volume:131; issue:3; firstpage:818; lastpage:828; numberofpages:11; journal:BRAIN; http://hdl.handle.net/11577/3354319Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-39749121457

الإتاحة: https://doi.org/10.1093/brain/awn007Test
http://hdl.handle.net/11577/3354319Test

المؤلفون: Tzoulis C., Engelsen B. A., Telstad W., Aasly J., Zeviani M., Winterthun S., Ferrari G., Aarseth J. H., Bindoff L. A.

المساهمون: Tzoulis, C., Engelsen, B. A., Telstad, W., Aasly, J., Zeviani, M., Winterthun, S., Ferrari, G., Aarseth, J. H., Bindoff, L. A.

مصطلحات موضوعية: Alper, Ataxia, Hepatic, Mitochondrial, POLG, Adolescent, Adult, Age of Onset, Aged, Child, DNA Polymerase gamma, DNA, DNA-Directed DNA Polymerase, Developmental Disabilitie, Diffuse Cerebral Sclerosis of Schilder, Disease Progression, Epidemiologic Method, Epilepsy, Tonic-Clonic, Female, Genotype, Heredodegenerative Disorders, Nervous System, Human, Liver Failure, Magnetic Resonance Imaging, Male, Middle Aged, Mitochondrial Disease, Mutation

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/16638794; info:eu-repo/semantics/altIdentifier/wos/WOS:000238761200012; volume:129; issue:7; firstpage:1685; lastpage:1692; numberofpages:8; journal:BRAIN; http://hdl.handle.net/11577/3354339Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-33745685519

الإتاحة: https://doi.org/10.1093/brain/awl097Test
http://hdl.handle.net/11577/3354339Test

المؤلفون: Ross, O. A., Soto-Ortolaza, A. I., Heckman, M. G., Aasly, J. O., Abahuni, N., Annesi, G., Bacon, J. A., Bardien, S., Bozi, M., Brice, A., Brighina, L., Van Broeckhoven, C., Carr, J., Chartier-Harlin, M. C., Dardiotis, E., Dickson, D. W., Diehl, N. N., Elbaz, A., Ferrarese, C., Ferraris, A., Fiske, B., Gibson, J. M., Gibson, R., Hadjigeorgiou, G. M., Hattori, N., Ioannidis, J. P., Jasinska-Myga, B., Jeon, B. S., Kim, Y. J., Klein, C., Kruger, R., Kyratzi, E., Lesage, S., Lin, C. H., Lynch, T., Maraganore, D. M., Mellick, G. D., Mutez, E., Nilsson, C., Opala, G., Park, S. S., Puschmann, A., Quattrone, A., Sharma, M., Silburn, P. A., Sohn, Y. H., Stefanis, L., Tadic, V., Theuns, J., Tomiyama, H., Uitti, R. J., Valente, E. M., van de Loo, S., Vassilatis, D. K., Vilarino-Guell, C., White, L. R., Wirdefeldt, K., Wszolek, Z. K., Wu, R. M., Farrer, M. J.

مصطلحات موضوعية: Adolescent, Adult, Aged, 80 and over, Case-Control Studies, Ethnic Groups/genetics, Exons/*genetics, Female, Gene Frequency, Genetic Predisposition to Disease, Genome-Wide Association Study/methods, Genotype, Humans, International Cooperation, Male, Middle Aged, Parkinson Disease/*genetics, Polymorphism, Single Nucleotide/*genetics, Protein-Serine-Threonine Kinases/*genetics, Risk Factors, Young Adult

العلاقة: http://olympias.lib.uoi.gr/jspui/handle/123456789/23652Test

الإتاحة: http://olympias.lib.uoi.gr/jspui/handle/123456789/23652Test

المؤلفون: Cobb, S. A., Wider, C., Ross, O. A., Mata, I. F., Adler, C. H., Rajput, A., Rajput, A. H., Wu, R. M., Hauser, R., Josephs, K. A., Carr, J., Gwinn, K., Heckman, M. G., Aasly, J. O., Lynch, T., Uitti, R. J., Wszolek, Z. K., Kapatos, G., Farrer, M. J.

مصطلحات موضوعية: cytosine, DJ 1 protein, gene product, guanine, guanosine triphosphate cyclohydrolase I, parkin, protein pink1, unclassified drug, adolescent, adult, article, controlled study, dystonia, female, gene deletion, gene duplication, gene frequency, gene locus, gene sequence, genetic variability, heterozygote, homozygote, human, major clinical study, male, mutation rate, onset age, Parkinson disease, priority journal, single nucleotide polymorphism

العلاقة: Movement Disorders; 24; 14; http://hdl.handle.net/10019.1/14206Test

الإتاحة: https://doi.org/10.1002/mds.22729Test
http://hdl.handle.net/10019.1/14206Test

المؤلفون: Heckman, Michael G, Elbaz, Alexis, Brighina, Laura, Pastor, Pao, Payami, Haydeh, Pchelina, Sofya N, Petersen, Maria Skaalum, Puschmann, Andrea, Ritz, Beate, Rogaeva, Ekaterina, Sazci, Ali, Slawek, Jaroslaw, Stefanis, Leonidas, Chartier-Harlin, Marie-Christine, Tan, Eng-King, Toda, Tatsushi, Toft, Mathias, Van Broeckhoven, Christine, Wirdefeldt, Karin, Woitalla, Dirk, Wszolek, Zbigniew K, Zimprich, Alexander, Dardiotis, Efthimios, Destée, Alain, Ferrarese, Carlo, Ferraris, Alessandro, Fiske, Brian, Gispert, Suzana, Hadjigeorgiou, Georgios M, Hattori, Nobutaka, Soto-Ortolaza, Alexandra I, Ioannidis, John P A, Jasinska-Myga, Barbara, Jeon, Beom S, Kim, Yun Joong, Klein, Christine, Kruger, Rejko, Kyratzi, Elli, Lin, Chin-Hsien, Lohmann, Katja, Loriot, Marie-Anne, Serie, Daniel J, Lynch, Timothy, Mellick, George D, Mutez, Eugénie, Opala, Grzegorz, Park, Sung Sup, Petrucci, Simona, Quattrone, Aldo, Sharma, Manu, Silburn, Peter A, Sohn, Young Ho, Aasly, Jan O, Tadic, Vera, Tomiyama, Hiroyuki, Uitti, Ryan J, Valente, Enza Maria, Vassilatis, Demetrios K, Vilariño-Güell, Carles, White, Linda R, Annesi, Grazia, Wu, Ruey-Meei, Xiromerisiou, Georgia, Maraganore, Demetrius M, Farrer, Matthew J, Ross, Owen A, Disease, Genetic Epidemiology Of Parkinson's, Auburger, Georg, Ioannidis, John P, Annesi, Grazie, Bentivoglio, Annarita, Bozi, Maria, Brice, Alexis, Carmine-Belin, Andrea, Carr, Jonathan, Bacon, Justin A, Carroll, Camille, Chase, Bruce, Checkoway, Harvey, Chen, Sheng-Di, Chung, Sun Ju, Cosentino, Carlos, Cresswell, Silke, Deutschlaender, Angela, Boczarska-Jedynak, Magdalena, Foroud, Tatiana, Garraux, Gaëtan, Goldwurm, Stefano, Hadjigeorgiou, George, Jeon, Beom Seok, Kawakami, Hideshi, Kishore, Asha, Krainc, Dimitri, Krygowska-Wajs, Anna, Lay-Son, Luis, Lin, Jeui-Jueng, Mellick, George, Morrison, Karen E, Munhoz, Renato P, Okubadejo, Njide U

المساهمون: Van Broeckhoven, Christine, Heckman, M, Elbaz, A, Soto Ortolaza, A, Serie, D, Aasly, J, Annesi, G, Auburger, G, Bacon, J, Boczarska Jedynak, M, Bozi, M, Brighina, L, Chartier Harlin, M, Dardiotis, E, Destée, A, Ferrarese, C, Ferraris, A, Fiske, B, Gispert, S, Hadjigeorgiou, G, Hattori, N, Ioannidis, J, Jasinska Myga, B, Jeon, B, Kim, Y, Klein, C, Kruger, R, Kyratzi, E, Lin, C, Lohmann, K, Loriot, M, Lynch, T, Mellick, G, Mutez, E, Opala, G, Park, S, Petrucci, S, Quattrone, A, Sharma, M, Silburn, P, Sohn, Y, Stefanis, L, Tadic, V, Tomiyama, H, Uitti, R, Valente, E, Vassilatis, D, Vilariño Güell, C, White, L, Wirdefeldt, K, Wszolek, Z, Wu, R, Xiromerisiou, G, Maraganore, D, Farrer, M, Ross, O

المصدر: Neurobiology of aging 35(1), 266.e5-266.e14 (2014). doi:10.1016/j.neurobiolaging.2013.07.013
Neurobiology of aging

مصطلحات موضوعية: Male, Aging, Parkinson's disease, european continental ancestry group, chemistry.chemical_compound, genetics [Parkinson Disease], Genotype, 80 and over, MAPT, genetics, genetics [Genetic Predisposition to Disease], Genetics, Aged, 80 and over, biology, General Neuroscience, LRRK2, Parkinson Disease, Middle Aged, Protein-Serine-Threonine Kinases, genetics [European Continental Ancestry Group], genetics [alpha-Synuclein], alpha-Synuclein, Medical genetics, Female, interaction, lrrk2, mapt, parkinson's disease, snca, adolescent, adult, aged, aged, 80 and over, asian continental ancestry group, female, genetic predisposition to disease, genotype, haplotypes, humans, leucine-rich repeat serine-threonine protein kinase-2, male, middle aged, parkinson disease, protein-serine-threonine kinases, risk, young adult, alpha-synuclein, tau proteins, genetic variation, Adult, Risk, medicine.medical_specialty, Interaction, Adolescent, Tau protein, MAPT protein, human, tau Proteins, Protein Serine-Threonine Kinases, Leucine-Rich Repeat Serine-Threonine Protein Kinase-2, genetics [Protein-Serine-Threonine Kinases], White People, Article, Young Adult, Genetic, Asian People, Genetic variation, genetics [Haplotypes], medicine, Humans, Genetic Predisposition to Disease, ddc:610, LRRK2 protein, human, SNCA protein, human, Biology, Aged, Alpha-synuclein, genetics [Asian Continental Ancestry Group], Haplotype, Genetic Variation, medicine.disease, nervous system diseases, genetics [tau Proteins], Haplotypes, chemistry, biology.protein, prevention & control [Parkinson Disease], SNCA, Neurology (clinical), Human medicine, Geriatrics and Gerontology, Developmental Biology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a89d123fd093770f9b70adf4f21ecf7Test
https://pub.dzne.de/record/137120Test